Canonical Allele Identifier: CA398382104

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999895-C-A
• MyVariant Identifiers: chr17:g.15903209C>A (hg19) ; chr17:g.15999895C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999895C>A , CM000679.2:g.15999895C>A	GRCh38
NC_000017.10:g.15903209C>A , CM000679.1:g.15903209C>A	GRCh37
NC_000017.9:g.15843934C>A	NCBI36
NG_029806.1:g.5516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.47C>A MANE Select	ENSP00000261647.5:p.Ala16Asp
ENST00000261647.9:c.47C>A	ENSP00000261647.5:p.Ala16Asp
ENST00000466729.5:c.112C>A
ENST00000470399.1:c.62C>A	ENSP00000465082.1:p.Ala21Asp
ENST00000475723.5:c.94C>A
ENST00000497842.6:n.72C>A
ENST00000583704.1:n.72C>A
NM_001271420.1:c.-412C>A	NP_001258349.1:n.-412C>A
NM_017775.3:c.47C>A	NP_060245.3:p.Ala16Asp
XM_011523950.1:c.47C>A	XP_011522252.1:p.Ala16Asp
XM_017024801.2:c.47C>A	XP_016880290.2:p.Ala16Asp
XM_017024802.2:c.47C>A	XP_016880291.2:p.Ala16Asp
XM_024450814.1:c.47C>A	XP_024306582.1:p.Ala16Asp
NM_017775.4:c.47C>A MANE Select	NP_060245.3:p.Ala16Asp
NM_001271420.2:c.-412C>A	NP_001258349.1:n.-412C>A